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从健康供体中鉴定出的英夫利昔单抗和利妥昔单抗的CD4 T细胞表位的特性分析

Characterization of CD4 T Cell Epitopes of Infliximab and Rituximab Identified from Healthy Donors.

作者信息

Hamze Moustafa, Meunier Sylvain, Karle Anette, Gdoura Abdelaziz, Goudet Amélie, Szely Natacha, Pallardy Marc, Carbonnel Franck, Spindeldreher Sebastian, Mariette Xavier, Miceli-Richard Corinne, Maillère Bernard

机构信息

CEA-Saclay, Institut de Biologie et Technologies, Université Paris-Saclay, Gif sur Yvette, France.

Novartis Pharma AG, Basel, Switzerland.

出版信息

Front Immunol. 2017 May 5;8:500. doi: 10.3389/fimmu.2017.00500. eCollection 2017.

Abstract

The chimeric antibodies anti-CD20 rituximab (Rtx) and anti-TNFα infliximab (Ifx) induce antidrug antibodies (ADAs) in many patients with inflammatory diseases. Because of the key role of CD4 T lymphocytes in the initiation of antibody responses, we localized the CD4 T cell epitopes of Rtx and Ifx. With the perspective to anticipate immunogenicity of therapeutic antibodies, identification of the CD4 T cell epitopes was performed using cells collected in healthy donors. Nine T cell epitopes were identified in the variable chains of both antibodies by deriving CD4 T cell lines raised against either Rtx or Ifx. The T cell epitopes often exhibited a good affinity for human leukocyte antigen (HLA)-DR molecules and were part of the peptides identified by MHC-associated peptide proteomics assay from HLA-DR molecules of dendritic cells (DCs) loaded with the antibodies. Two-third of the T cell epitopes identified from the healthy donors stimulated peripheral blood mononuclear cells from patients having developed ADAs against Rtx or Ifx and promoted the secretion of a diversity of cytokines. These data emphasize the predictive value of evaluating the T cell repertoire of healthy donors and the composition of peptides bound to HLA-DR of DCs to anticipate and prevent immunogenicity of therapeutic antibodies.

摘要

嵌合抗体抗CD20利妥昔单抗(Rtx)和抗TNFα英夫利昔单抗(Ifx)在许多炎症性疾病患者中会诱导产生抗药抗体(ADA)。由于CD4 T淋巴细胞在抗体应答启动中起关键作用,我们定位了Rtx和Ifx的CD4 T细胞表位。为了预测治疗性抗体的免疫原性,利用健康供体采集的细胞对CD4 T细胞表位进行了鉴定。通过培养针对Rtx或Ifx的CD4 T细胞系,在两种抗体的可变链中鉴定出9个T细胞表位。这些T细胞表位通常对人类白细胞抗原(HLA)-DR分子具有良好的亲和力,并且是通过MHC相关肽蛋白质组学分析从负载抗体的树突状细胞(DC)的HLA-DR分子中鉴定出的肽段的一部分。从健康供体中鉴定出的T细胞表位中有三分之二能刺激已产生针对Rtx或Ifx的ADA的患者的外周血单核细胞,并促进多种细胞因子的分泌。这些数据强调了评估健康供体的T细胞库以及与DC的HLA-DR结合的肽段组成以预测和预防治疗性抗体免疫原性的预测价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bcc/5418239/3adc98ae63d2/fimmu-08-00500-g001.jpg

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